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Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report

The fibrous dysplasia of bone is painless, benign, and slowly progressive bone lesion. It may rarely become aggressive by compression of adjacent organs or malignant transformation. This disease falls within the scope of a McCune-Albright syndrome in less than 7 % of cases. The authors reported the...

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Detalles Bibliográficos
Autores principales: Bile-Gui, Lynda N., Ahoury, Judicael, Kabas, Raïssa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569405/
https://www.ncbi.nlm.nih.gov/pubmed/33102631
http://dx.doi.org/10.1016/j.ejro.2019.12.002
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author Bile-Gui, Lynda N.
Ahoury, Judicael
Kabas, Raïssa M.
author_facet Bile-Gui, Lynda N.
Ahoury, Judicael
Kabas, Raïssa M.
author_sort Bile-Gui, Lynda N.
collection PubMed
description The fibrous dysplasia of bone is painless, benign, and slowly progressive bone lesion. It may rarely become aggressive by compression of adjacent organs or malignant transformation. This disease falls within the scope of a McCune-Albright syndrome in less than 7 % of cases. The authors reported the case of a 25-year-old woman, living in the countryside, who suffered from a severe craniofacial fibrous dysplasia which has begun since her childhood with no medical care. Her clinical picture was that of McCune-Albright syndrome, and CT scan revealed advanced dysplasia with endocranial compression.
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spelling pubmed-75694052020-10-23 Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report Bile-Gui, Lynda N. Ahoury, Judicael Kabas, Raïssa M. Eur J Radiol Open Article The fibrous dysplasia of bone is painless, benign, and slowly progressive bone lesion. It may rarely become aggressive by compression of adjacent organs or malignant transformation. This disease falls within the scope of a McCune-Albright syndrome in less than 7 % of cases. The authors reported the case of a 25-year-old woman, living in the countryside, who suffered from a severe craniofacial fibrous dysplasia which has begun since her childhood with no medical care. Her clinical picture was that of McCune-Albright syndrome, and CT scan revealed advanced dysplasia with endocranial compression. Elsevier 2020-01-28 /pmc/articles/PMC7569405/ /pubmed/33102631 http://dx.doi.org/10.1016/j.ejro.2019.12.002 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Bile-Gui, Lynda N.
Ahoury, Judicael
Kabas, Raïssa M.
Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report
title Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report
title_full Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report
title_fullStr Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report
title_full_unstemmed Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report
title_short Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report
title_sort imaging of advanced craniofacial fibrous dysplasia associated with mccune-albright syndrome: a case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569405/
https://www.ncbi.nlm.nih.gov/pubmed/33102631
http://dx.doi.org/10.1016/j.ejro.2019.12.002
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